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Origins and functional impact of copy number variation in the human genome
Epigenetics makes cancer cell “lean mean machine”
The Wellcome Trust Case Control Consortium, Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Candidate malaria susceptibility/protective SNPs in hospital and population-based studies: the effect of sub-structuring
Consolidation of the cancer genome into domains of repressive chromatin by long-range epigenetic silencing (LRES) reduces transcriptional plasticity.
KCNN4 Gene variant is associated with ileal CrohnÂ´s disease in the Australian and New Zealand population
Genetic analysis of six SNPs in candidate genes associated with high cross-race risk of development of thoracic aortic aneurysms and dissections in Chinese Han population
Testing replication of a 5-SNP set for general cognitive ability in six population samples
Genome-wide scan identifies a quantitative trait locus at 4p15.3 for serum urate
Association between single-nucleotide polymorphism in Mal/TIRAP and Interleukin-10 genes and susceptibility to invasive Haemophilus influenzea serotype b infection in immunized children